Reconstructing ancient ocean redox conditions is essential for understanding the link between marine anoxia and environmental changes. The Early Jurassic experienced significant oceanic redox fluctuations during the Pliensbachian/Toarcian event (Pl/To; ~184 Ma) and the more pronounced Toarcian Oceanic Anoxic Event (T-OAE; ~183 Ma). However, the expansion and connectivity of anoxic waters, e.g., in the European epicontinental seaways (EES), remain poorly understood. Here, we aim to apply U and Mo isotopes on carbonates and black shales that have become a powerful geochemical proxy for tracking redox changes at both local and global scales, combined with other redox-sensitive trace elements and REY, to unravel the oceanic redox evolution of the Early Jurassic.
Carbonate sediments investigated here are from Peniche (Portugal) and Toumliline (Morocco), covering both the Pl/To and T-OAE intervals. Shale-normalized rare earth element and yttrium patterns in the Peniche samples are characterized by negative Ce, positive Gd, and positive Y anomalies, indicating precipitation from open marine seawater. Recent data from near-contemporaneous Italian carbonate deposits suggest more extensive global seafloor anoxia during the T-OAE [1]. Our preliminary data, however, do not show negative U isotope shifts in the Peniche section suggesting that there was no global expansion of seafloor anoxia during either the Pl/To event or the T-OAE. Complementary U data of the Morocco section and coupled Mo-U isotope data from three different basins of the EES may clarify whether the redox shifts occurred contemporaneously and whether they represent a local or global phenomenon.
[1] Remírez et al. (2024), PNAS, 121(27)